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HS Code |
273793 |
| Chemical Name | 5,8-Dihydroxy-1,4-Naphthoquinone |
| Molecular Formula | C10H6O4 |
| Molar Mass | 190.15 g/mol |
| Appearance | Yellow to orange crystalline powder |
| Melting Point | 264-266 °C |
| Boiling Point | Decomposes |
| Solubility In Water | Slightly soluble |
| Cas Number | 82-86-0 |
| Structure | Naphthoquinone core with hydroxyl groups at positions 5 and 8 |
| Synonyms | Juglone |
| Pubchem Cid | 10216 |
| Density | 1.581 g/cm³ |
As an accredited 5,8-Dihydroxy-1,4-Naphthoquinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5,8-Dihydroxy-1,4-Naphthoquinone (10g) is packaged in a sealed amber glass bottle with a tamper-evident cap. |
| Shipping | 5,8-Dihydroxy-1,4-naphthoquinone is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Standard packaging meets regulatory requirements for chemical transport. The chemical is labeled with proper hazard and handling information, ensuring safe transit by ground or air according to local and international shipping regulations (e.g., DOT, IATA, IMDG). |
| Storage | 5,8-Dihydroxy-1,4-naphthoquinone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature or as indicated on the supplier’s label. Avoid excessive heat and sources of ignition to maintain stability and prevent decomposition. |
Applications of 5,8-Dihydroxy-1,4-Naphthoquinone in Industrial ManufacturingAs a specialty manufacturer of 5,8-Dihydroxy-1,4-Naphthoquinone (commonly known as Lawsone), we support industrial customers across several established sectors requiring high-purity intermediate chemicals. Below, we detail the principal downstream use cases, specifying precise industry standards, functional dosage guidelines, integration within manufacturing sequences, and the final product formats produced by our clients. 1. Hair Dye Ingredient ProductionHair color formulators in the cosmetics sector rely on this quinone exclusively for the synthesis of natural-origin and permanent hair dyes, leveraging its molecular affinity for keratin and direct dyeing capability. Precise control of concentration allows tailored color intensity and stability during blending with oxidants or other dye precursors. Manufacturers optimize dye shade and fastness through managed pH and selection of compatible coupling agents in batch or continuous processes that demand careful quality monitoring. The resulting finished goods occupy premium and natural hair treatment markets worldwide. Industry compliance standards
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2. Biologically-Derived Textile Dye ManufactureTextile dyeing plants incorporate the compound as a core coloring agent for eco-friendly cellulosic and protein fiber dyeing systems, selecting it for its strong affinity with cotton, wool, and silk substrates. Dosage precision aligns chroma uniformity and wash fastness, while compliance testing assures safe residual limits on finished fabrics. Dyeing occurs in jet, pad-batch, or exhaust systems during the wet processing sequences; color adjustment is achieved through modifiers and controlled reaction times under regulated thermal conditions. Licit downstream imports often demand transparent traceability and certification. Industry compliance standards
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3. Pharmaceutical Intermediate for Vitamin K SynthesisThis naphthoquinone serves as a validated chemical synthon in regulated Active Pharmaceutical Ingredient (API) manufacturing, particularly for menadione (vitamin K3) and related analogues. API manufacturers use it in sequence-specific steps that involve selective reduction, methylation, or condensation reactions, often within GMP-certified environments. Dialed production purity minimizes side-reactions and meets pharmacopoeial specifications for downstream drug or supplement formulation. Industry compliance standards
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4. Organic Electronic Materials & Conductive Pigment FormulationAdvanced manufacturers leverage the electron-accepting properties of this compound in formulating conductive polymers, printable electronic inks, and as a functional pigment in organic electronic components. The raw material delivers controlled charge transport and color performance in flexible thin-film applications, requiring careful blending with carriers and stabilizers. Use concentrations vary by substrate compatibility and device design, and industrial quality checks validate batch-to-batch consistency, alignment with purity specifications, and electrochemical stability suitable for downstream assembly. Industry compliance standards
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5. Analytical Reagents for Metal Detection and ResearchLaboratory and industrial reagent producers use the compound as a chromogenic agent in complexometric titration kits, and as a precursor for specialty detection reagents in analytical chemistry. Its selective chelating properties enable colorimetric assays for various metal ions in environmental, food, and industrial water testing. Production processes require stringent QC and validation against reference materials to ensure diagnostic reliability and repeatable quantification thresholds. Variability in formulation reflects the metal specificity and sensitivity required for each assay. Industry compliance standards
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